Capsinac
Product Images NDC 73247-201

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Capsinac (NDC 73247-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bodysphere, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Capsinac 01)

Chemical structure of the active ingredient shown for Capsinac, depicting a molecule with two chlorine atoms attached to a benzene ring and a sodium carboxylate group.*

FDA Label Image

Figure A (Capsinac 02)

An instructional illustration labeled 'Figure A' showing two methods of using a liquid product: one hand is shown tilting a bottle and pouring liquid into the palm of the opposite hand, and the other depicts pouring onto a bent knee. The drawings emphasize administration technique without text details.*

FDA Label Image

Figure B (Capsinac 03)

An instructional illustration showing a hand applying a topical product to the front of a knee. Arrows indicate a downward and circular motion on the knee area, demonstrating the application technique.*

FDA Label Image

Figure C (Capsinac 04)

An instructional illustration showing a hand applying a substance to the skin on a forearm using circular motions, indicated by an arrow. The image likely demonstrates proper topical application technique for a medication like Capsinac.*

FDA Label Image

Principal Display Panel (Kit Carton)

Capsinac Therapy Kit label displaying the product name and logo prominently. The kit contains Diclofenac Sodium Topical Solution (1.5% w/w, 5 fl oz/150 mL) and Capsaicin Cream (0.025%, 8 fl oz/237 mL). The label lists active and inactive ingredients, including diclofenac sodium and capsaicin, and notes the product is for topical use only. It includes the NDC 73247-201-01 and identifies Bodysphere, LLC as the labeler.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.